Reductive deamination of aromatic amines with nitric oxide (NO)

Takashi Itoh; Yûji Matsuya; Kazuhiro Nagata; Akio Ohsawa

doi:10.1016/0040-4039(96)00785-X

Reductive deamination of aromatic amines with nitric oxide (NO)

Takashi Itoh, Yûji Matsuya, Kazuhiro Nagata, Akio Ohsawa^*

^*Corresponding author for this work

Synthetic and Medicinal Chemistry

Research output: Contribution to journal › Article › peer-review

29 Scopus citations

Abstract

Aromatic amines were treated with nitric oxide in tetrahydrofuran or chloroform under argon atmosphere to afford deaminated aromatic compounds in good yields. The reaction is suggested to proceed via aryl radicals, which are supposed to be formed by reduction of aryldiazonium salts with NO.

Original language	English
Pages (from-to)	4165-4168
Number of pages	4
Journal	Tetrahedron Letters
Volume	37
Issue number	24
DOIs	https://doi.org/10.1016/0040-4039(96)00785-X
State	Published - 1996/06/10

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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title = "Reductive deamination of aromatic amines with nitric oxide (NO)",

abstract = "Aromatic amines were treated with nitric oxide in tetrahydrofuran or chloroform under argon atmosphere to afford deaminated aromatic compounds in good yields. The reaction is suggested to proceed via aryl radicals, which are supposed to be formed by reduction of aryldiazonium salts with NO.",

author = "Takashi Itoh and Y{\^u}ji Matsuya and Kazuhiro Nagata and Akio Ohsawa",

year = "1996",

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T1 - Reductive deamination of aromatic amines with nitric oxide (NO)

AU - Itoh, Takashi

AU - Matsuya, Yûji

AU - Nagata, Kazuhiro

AU - Ohsawa, Akio

PY - 1996/6/10

Y1 - 1996/6/10

N2 - Aromatic amines were treated with nitric oxide in tetrahydrofuran or chloroform under argon atmosphere to afford deaminated aromatic compounds in good yields. The reaction is suggested to proceed via aryl radicals, which are supposed to be formed by reduction of aryldiazonium salts with NO.

AB - Aromatic amines were treated with nitric oxide in tetrahydrofuran or chloroform under argon atmosphere to afford deaminated aromatic compounds in good yields. The reaction is suggested to proceed via aryl radicals, which are supposed to be formed by reduction of aryldiazonium salts with NO.

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U2 - 10.1016/0040-4039(96)00785-X

DO - 10.1016/0040-4039(96)00785-X

M3 - 学術論文

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SN - 0040-4039

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EP - 4168

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 24

ER -

Reductive deamination of aromatic amines with nitric oxide (NO)

Abstract

ASJC Scopus subject areas

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